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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Other And Unspecified Congenital Anomalies 759.* >

2007 ICD-9-CM Diagnosis 759.9

Congenital anomaly unspecified

 On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date.

The 2009 version of ICD-9-CM 759.9 can be accessed here.

  • Congenital malformations of organs or parts.
  • 759.9 is a specific code that can be used to specify a diagnosis
  • 759.9 contains 18 index entries
  • View the ICD-9-CM Volume 1 759.* hierarchy

Index entries containing 759.9:

Abnormal, abnormality, abnormalities - see also Anomaly
  • anatomical relationship NEC 759.9
  • development, developmental NEC 759.9
Anomaly, anomalous (congenital) (unspecified type) 759.9Defect, defective 759.9
  • 3-beta-hydroxysteroid dehydrogenase 255.2
  • 11-hydroxylase 255.2
  • 21-hydroxylase 255.2
  • abdominal wall, congenital 756.70
  • aorticopulmonary septum 745.0
  • aortic septal 745.0
  • atrial septal (ostium secundum type) 745.5
  • atrioventricular
  • atrium secundum 745.5
  • auricular septal 745.5
  • bilirubin excretion 277.4
  • biosynthesis, testicular androgen 257.2
  • bridge 525.60
  • bulbar septum 745.0
  • butanol-insoluble iodide 246.1
  • chromosome - see Anomaly, chromosome
  • circulation (acquired) 459.9
  • clotting NEC (see also Defect, coagulation) 286.9
  • coagulation (factor) (see also Deficiency, coagulation factor) 286.9
    • with
      • abortion - see Abortion, by type, with hemorrhage
      • ectopic pregnancy (see also categories 634-638) 639.1
      • molar pregnancy (see also categories 630-632) 639.1
    • acquired (any) 286.7
    • antepartum or intrapartum 641.3
      • affecting fetus or newborn 762.1
    • causing hemorrhage of pregnancy or delivery 641.3
    • complicating pregnancy, childbirth, or puerperium 649.3
    • due to
    • newborn, transient 776.3
    • postpartum 666.3
    • specified type NEC 286.3
  • conduction (heart) 426.9
    • bone (see also Deafness, conductive) 389.00
  • congenital, organ or site NEC - see also Anomaly
  • crown 525.60
  • cushion endocardial 745.60
  • dental restoration 525.60
  • dentin (hereditary) 520.5
  • Descemet's membrane (congenital) 743.9
  • deutan 368.52
  • developmental - see also Anomaly, by site
    • cauda equina 742.59
    • left ventricle 746.9
      • with atresia or hypoplasia of aortic orifice or valve, with hypoplasia of ascending aorta 746.7
      • in hypoplastic left heart syndrome 746.7
    • testis 752.9
    • vessel 747.9
  • diaphragm
    • with elevation, eventration, or hernia - see Hernia, diaphragm
    • congenital 756.6
      • with elevation, eventration, or hernia 756.6
      • gross (with elevation, eventration, or hernia) 756.6
  • ectodermal, congenital 757.9
  • Eisenmenger's (ventricular septal defect) 745.4
  • endocardial cushion 745.60
  • esophagus, congenital 750.9
  • extensor retinaculum 728.9
  • fibrin polymerization (see also Defect, coagulation) 286.3
  • filling
  • fossa ovalis 745.5
  • gene, carrier (suspected) of V83.89
  • Gerbode 745.4
  • glaucomatous, without elevated tension 365.89
  • Hageman (factor) (see also Defect, coagulation) 286.3
  • hearing (see also Deafness) 389.9
  • high grade 317
  • homogentisic acid 270.2
  • interatrial septal 745.5
  • interauricular septal 745.5
  • interventricular septal 745.4
    • with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle 745.2
    • acquired 429.71
    • in tetralogy of Fallot 745.2
  • iodide trapping 246.1
  • iodotyrosine dehalogenase 246.1
  • kynureninase 270.2
  • learning, specific 315.2
  • major osseous 731.3
  • mental (see also Retardation, mental) 319
  • osseous, major 731.3
  • osteochondral NEC 738.8
  • ostium
  • pericardium 746.89
  • peroxidase-binding 246.1
  • placental blood supply - see Placenta, insufficiency
  • platelet (qualitative) 287.1
  • postural, spine 737.9
  • protan 368.51
  • pulmonic cusps, congenital 746.00
  • renal pelvis 753.9
  • respiratory system, congenital 748.9
  • retina, retinal 361.30
  • septal (closure) (heart) NEC 745.9
  • speech NEC 784.5
  • Taussig-Bing (transposition, aorta and overriding pulmonary artery) 745.11
  • teeth, wedge 521.20
  • thyroid hormone synthesis 246.1
  • tritan 368.53
  • ureter 753.9
  • vascular (acquired) (local) 459.9
  • ventricular septal 745.4
    • with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle 745.2
    • acquired 429.71
    • atrioventricular canal type 745.69
    • between infundibulum and anterior portion 745.4
    • in tetralogy of Fallot 745.2
    • isolated anterior 745.4
  • vision NEC 369.9
  • visual field 368.40
  • voice 784.40
  • wedge, teeth (abrasion) 521.20
Deformity 738.9
  • abdomen, congenital 759.9
  • congenital, organ or site not listed (see also Anomaly) 759.9
  • lymphatic system, congenital 759.9
  • trunk (acquired) 738.3
    • congenital 759.9
Embryopathia NEC 759.9
Malformation (congenital) - see also Anomaly
  • umbilicus 759.9